US6033683A - Method of the manufacture of suppositories - Google Patents
Method of the manufacture of suppositories Download PDFInfo
- Publication number
- US6033683A US6033683A US08/666,543 US66654396A US6033683A US 6033683 A US6033683 A US 6033683A US 66654396 A US66654396 A US 66654396A US 6033683 A US6033683 A US 6033683A
- Authority
- US
- United States
- Prior art keywords
- suppositories
- carbon dioxide
- process according
- fatty
- mixture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000829 suppository Substances 0.000 title claims abstract description 25
- 238000000034 method Methods 0.000 title claims abstract description 22
- 238000004519 manufacturing process Methods 0.000 title description 12
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims abstract description 38
- 229910002092 carbon dioxide Inorganic materials 0.000 claims abstract description 19
- 239000001569 carbon dioxide Substances 0.000 claims abstract description 19
- 230000008569 process Effects 0.000 claims abstract description 18
- 239000000126 substance Substances 0.000 claims abstract description 13
- 238000003756 stirring Methods 0.000 claims abstract description 10
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims abstract description 7
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- 235000010445 lecithin Nutrition 0.000 claims abstract description 7
- 229940067606 lecithin Drugs 0.000 claims abstract description 7
- 239000000787 lecithin Substances 0.000 claims abstract description 7
- 235000016337 monopotassium tartrate Nutrition 0.000 claims abstract description 6
- KYKNRZGSIGMXFH-ZVGUSBNCSA-M potassium bitartrate Chemical compound [K+].OC(=O)[C@H](O)[C@@H](O)C([O-])=O KYKNRZGSIGMXFH-ZVGUSBNCSA-M 0.000 claims abstract description 6
- 239000000725 suspension Substances 0.000 claims abstract description 6
- 239000000470 constituent Substances 0.000 claims abstract description 5
- 239000012530 fluid Substances 0.000 claims abstract description 5
- 238000002844 melting Methods 0.000 claims abstract description 5
- 230000008018 melting Effects 0.000 claims abstract description 5
- 235000013311 vegetables Nutrition 0.000 claims abstract description 5
- 238000001033 granulometry Methods 0.000 claims abstract description 4
- 229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 3
- 239000011707 mineral Substances 0.000 claims abstract description 3
- 238000002360 preparation method Methods 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 11
- 150000003626 triacylglycerols Chemical class 0.000 claims description 6
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 4
- -1 alkali metal bicarbonate Chemical class 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 claims description 4
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 3
- 238000007711 solidification Methods 0.000 claims description 3
- 230000008023 solidification Effects 0.000 claims description 3
- 239000008347 soybean phospholipid Substances 0.000 claims description 3
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 235000019359 magnesium stearate Nutrition 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 239000004408 titanium dioxide Substances 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical class [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 239000000155 melt Substances 0.000 claims 1
- 239000004033 plastic Substances 0.000 claims 1
- 229920003023 plastic Polymers 0.000 claims 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 abstract description 8
- 229910000030 sodium bicarbonate Inorganic materials 0.000 abstract description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 abstract description 4
- 230000002475 laxative effect Effects 0.000 abstract description 3
- 235000010755 mineral Nutrition 0.000 abstract description 2
- 239000003708 ampul Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 150000001552 barium Chemical class 0.000 description 1
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 1
- 229910002113 barium titanate Inorganic materials 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 238000003760 magnetic stirring Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 210000000664 rectum Anatomy 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 150000003608 titanium Chemical class 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0002—Galenical forms characterised by the drug release technique; Application systems commanded by energy
- A61K9/0007—Effervescent
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/02—Suppositories; Bougies; Bases therefor; Ovules
Definitions
- the present invention relates to the field of pharmacotechnology.
- Its subject is more especially a new process for the preparation of suppositories and in particular of suppositories having a laxative action.
- its subject is a process for the preparation of suppositories having a laxative action which are capable of causing a release of carbon dioxide by chemical reaction of active principles upon contact with the moisture present in the rectal ampul.
- a medicinal preparation using this process subsequently appeared on the market. It is formed of a suppository containing an effervescent mixture of potassium acid tartrate and sodium bicarbonate capable, in a moist environment, of releasing ca. 50 ml to 100 ml of carbon dioxide in the rectum.
- the active principles are not coated in an impermeable matrix, they are capable of reacting prematurely amongst themselves in the presentation pack and, above all, they are capable of reacting too violently amongst themselves in the rectal ampul and triggering distensions of the rectal ampul which are too great.
- the fatty substances are melted separately, the mixture is left to cool to the desired temperature and vegetable lecithin is dispersed in the fluid mass resulting from the melting, then a mineral opacifying agent is incorporated, and this is followed by the pouring in succession of the potassium acid tartrate, accompanied by stirring, and then of the sodium bicarbonate, accompanied by more vigorous stirring, these two constituents having a particular granulometry, and stirring is then continued until perfect homogeneity is achieved before proceeding with the drawing-off of the fluid suspension into the alveoli of suppositories.
- suppositories of a regular truncated-cone shape are obtained whose composition is homogeneous and whose preservation, attested by the volume of the release of carbon dioxide, is assured for at least two years.
- the technical problem to be solved is markedly different from that considered by the Waldenmeyer process.
- the fatty substances constituted a tight coating which protected completely, and even too completely, against the catalytic action of a hydrophilic agent and it was necessary to incorporate in it a product facilitating the passage of aqueous media.
- the excipients for suppositories are made from stearates of polyethylene glycol or triglycerides of fatty acids having a medium chain which are substances that are lipophilic and hydrophilic at one and the same time, so that it is necessary to protect the reactive substances of the mixture by an inert protective screen and no longer by lipoid substances.
- the fatty substances which act as a support for the realization of suppositories are triglycerides of fatty acids having a medium chain sold under the name Novata BD by the HENKEL company. Those sold under the name Estaram H15 by the UNICHEMA company or those sold under the name Suppocire AM by the GATTEFOSSE company, or those sold under the name Witepsol H 15 by the HULS company, can also be used. These triglycerides have a melting range from 35 to 39° C.
- Vegetable lecithin is a soya lecithin and in particular the type sold under the name Topcithin 50 by the LUCAS MEYER company or that sold under the name MC Thin AF1 by the same company.
- Lecithin makes it possible to avoid or reduce thickening of the mass before pouring and is used in the cases of solid active principles which partially solubilize or, above all, in the cases of powdery active principles. Depending on the circumstances, lecithin dissolves in the fatty substance or, on the contrary, remains in suspension.
- the opacifying agent is a natural or artificial silicate such as talc or magnesium silicate, or an alkaline-earth metal stearate such as calcium stearate or magnesium stearate, or a derivative of titanium such as titanium dioxide, or a derivative of barium such as barium titanate.
- the granulometry of the constituents of the effervescent mixture is adjusted in such a way that the powders have a great fineness and are distributed in a perfectly homogeneous manner without setting under stirring as the preparation proceeds.
- the temperature of the suppositories, after pouring into the alveoli, is progressively reduced by cooling until complete solidification.
- the thus-realized suppositories have a shelf life of two years, which guarantees their perservation for at least an equal period.
- the ingredients are left to mix for 10 minutes and then, while maintaining the temperature, the suspension is taken off and the alveoli are thus filled and passed into a cooling enclosure until solidification is complete.
- the suppository is quickly introduced into a test-tube A (100 ml) filled with water at 37° C. and the latter is closed with a fritted glass stopper (porosity 2) fitted with a rubber joint, while ensuring that no air bubbles are trapped.
- a fritted glass stopper porosity 2
- test-tube A is immersed in a second test-tube B (250 ml) filled with water at 37° C. and containing a magnetic bar.
- Test-tube B is placed in a water bath at ca. 40° C., arranged on a heating magnetic stirrer, so as to maintain a constant temperature (37° ⁇ 1° C.).
- the magnetic stirring and the heating are maintained throughout the gaseous release.
- the volume of carbon dioxide is read off from test-piece A.
- the average gaseous release is between 50 and 100 ml.
- the variations recorded take account at one and the same time of the difficulty of obtaining an absolutely homogeneous preparation and also the uncertain sensitivity of the methods of assessing the volume of gaseous release because of the solubility of carbon dioxide in water.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Mechanical Treatment Of Semiconductor (AREA)
- Compounds Of Unknown Constitution (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Liquid Crystal Substances (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9411913A FR2725371B1 (fr) | 1994-10-05 | 1994-10-05 | Nouveau procede de fabrication de suppositoires |
| FR9411913 | 1994-10-05 | ||
| PCT/FR1995/001294 WO1996010987A1 (fr) | 1994-10-05 | 1995-10-05 | Nouveau procede de fabrication de suppositoires |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US6033683A true US6033683A (en) | 2000-03-07 |
Family
ID=9467597
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US08/666,543 Expired - Lifetime US6033683A (en) | 1994-10-05 | 1995-10-05 | Method of the manufacture of suppositories |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US6033683A (pl) |
| EP (1) | EP0741564B1 (pl) |
| KR (1) | KR100384323B1 (pl) |
| CN (1) | CN1303983C (pl) |
| AT (1) | ATE322248T1 (pl) |
| BR (1) | BR9506439A (pl) |
| DE (1) | DE69534916T2 (pl) |
| FI (1) | FI119140B (pl) |
| FR (1) | FR2725371B1 (pl) |
| MX (1) | MX9602121A (pl) |
| NO (1) | NO317933B1 (pl) |
| PL (1) | PL183374B1 (pl) |
| WO (1) | WO1996010987A1 (pl) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000061748A1 (en) * | 1999-04-09 | 2000-10-19 | Human Genome Sciences, Inc. | 48 human secreted proteins |
| GB0818336D0 (en) | 2008-10-07 | 2008-11-12 | Cosmetic Warriors Ltd | Composition |
| CN105670003A (zh) * | 2014-11-21 | 2016-06-15 | 常州坤宇环保科技有限公司 | 高吸水树脂防结块剂 |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3764668A (en) * | 1970-09-30 | 1973-10-09 | Interx Research Corp | Compositions of salts of salicylamide |
| JPS55136215A (en) * | 1979-04-10 | 1980-10-23 | Res Inst For Prod Dev | Preparation of laminar laxative suppository |
| JPS5683417A (en) * | 1979-12-11 | 1981-07-08 | Kanae:Kk | Preparation of layer laxative suppository |
| EP0088394A2 (en) * | 1982-03-05 | 1983-09-14 | Eisai Co., Ltd. | Stable, effervescent vaginal suppository composition and suppositories made therefrom |
| EP0254693A1 (en) * | 1986-07-25 | 1988-01-27 | MED-IMPORT INTERNATIONAL S.r.l. | Pharmaceutical form for enteric administration of etodolic acid or its salts, in admixture with excipients |
| US5547976A (en) * | 1992-03-20 | 1996-08-20 | Burroughs Wellcome Co. | Further indole derivatives with antiviral activity |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR788198A (fr) * | 1934-12-18 | 1935-10-05 | Procédé pour la fabrication de préparations thérapeutiques dégageant de l'acide carbonique | |
| FR5391M (pl) * | 1965-11-04 | 1967-10-23 |
-
1994
- 1994-10-05 FR FR9411913A patent/FR2725371B1/fr not_active Expired - Fee Related
-
1995
- 1995-10-05 PL PL95314835A patent/PL183374B1/pl unknown
- 1995-10-05 EP EP95934170A patent/EP0741564B1/fr not_active Expired - Lifetime
- 1995-10-05 KR KR1019960702930A patent/KR100384323B1/ko not_active Expired - Lifetime
- 1995-10-05 WO PCT/FR1995/001294 patent/WO1996010987A1/fr not_active Ceased
- 1995-10-05 US US08/666,543 patent/US6033683A/en not_active Expired - Lifetime
- 1995-10-05 BR BR9506439A patent/BR9506439A/pt not_active Application Discontinuation
- 1995-10-05 DE DE69534916T patent/DE69534916T2/de not_active Expired - Lifetime
- 1995-10-05 AT AT95934170T patent/ATE322248T1/de not_active IP Right Cessation
- 1995-10-05 MX MX9602121A patent/MX9602121A/es unknown
- 1995-10-05 CN CNB951913565A patent/CN1303983C/zh not_active Expired - Fee Related
-
1996
- 1996-06-04 NO NO19962297A patent/NO317933B1/no not_active IP Right Cessation
- 1996-06-04 FI FI962328A patent/FI119140B/fi not_active IP Right Cessation
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3764668A (en) * | 1970-09-30 | 1973-10-09 | Interx Research Corp | Compositions of salts of salicylamide |
| JPS55136215A (en) * | 1979-04-10 | 1980-10-23 | Res Inst For Prod Dev | Preparation of laminar laxative suppository |
| JPS5683417A (en) * | 1979-12-11 | 1981-07-08 | Kanae:Kk | Preparation of layer laxative suppository |
| EP0088394A2 (en) * | 1982-03-05 | 1983-09-14 | Eisai Co., Ltd. | Stable, effervescent vaginal suppository composition and suppositories made therefrom |
| EP0254693A1 (en) * | 1986-07-25 | 1988-01-27 | MED-IMPORT INTERNATIONAL S.r.l. | Pharmaceutical form for enteric administration of etodolic acid or its salts, in admixture with excipients |
| US5547976A (en) * | 1992-03-20 | 1996-08-20 | Burroughs Wellcome Co. | Further indole derivatives with antiviral activity |
Non-Patent Citations (4)
| Title |
|---|
| Hakata et al. "Effects of Bases and Additives on Release of Carbon Dioxide from Effervescent Suppositories". Chem. Pharm. Bull., vol. 41, No. 2, pp 351-356, 1993. |
| Hakata et al. Effects of Bases and Additives on Release of Carbon Dioxide from Effervescent Suppositories . Chem. Pharm. Bull., vol. 41, No. 2, pp 351 356, 1993. * |
| Ijima et al. "Effects of Aerosil 200 and Soybean Lecithin on Release of Carbon Dioxide from Effervescent Suppositories". Yakuzaigaku, vol. 53, No. 1, pp 55-62, 1993. |
| Ijima et al. Effects of Aerosil 200 and Soybean Lecithin on Release of Carbon Dioxide from Effervescent Suppositories . Yakuzaigaku, vol. 53, No. 1, pp 55 62, 1993. * |
Also Published As
| Publication number | Publication date |
|---|---|
| BR9506439A (pt) | 1997-09-02 |
| FI962328L (fi) | 1996-06-04 |
| MX9602121A (es) | 1997-07-31 |
| ATE322248T1 (de) | 2006-04-15 |
| WO1996010987A1 (fr) | 1996-04-18 |
| NO317933B1 (no) | 2005-01-10 |
| DE69534916T2 (de) | 2007-03-08 |
| CN1139379A (zh) | 1997-01-01 |
| EP0741564B1 (fr) | 2006-04-05 |
| NO962297D0 (no) | 1996-06-04 |
| NO962297L (no) | 1996-06-04 |
| CN1303983C (zh) | 2007-03-14 |
| FR2725371A1 (fr) | 1996-04-12 |
| FI119140B (fi) | 2008-08-15 |
| PL183374B1 (pl) | 2002-06-28 |
| FI962328A0 (fi) | 1996-06-04 |
| EP0741564A1 (fr) | 1996-11-13 |
| PL314835A1 (en) | 1996-09-30 |
| KR960706324A (ko) | 1996-12-09 |
| KR100384323B1 (ko) | 2003-11-28 |
| FR2725371B1 (fr) | 1997-08-29 |
| DE69534916D1 (de) | 2006-05-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3374146A (en) | Sustained release encapsulation | |
| US4832956A (en) | Disintegrating tablet and process for its preparation | |
| US4371516A (en) | Articles for carrying chemicals | |
| US4013784A (en) | Delayed release pharmaceutical preparations | |
| US3138525A (en) | Castor wax-amprotropine-resin compositions | |
| US4127650A (en) | Medicinal simethicone containing composition and its method of production | |
| EA000434B1 (ru) | Фармацевтическая композиция, получаемая экструзией расплава | |
| EP0396972B2 (en) | An aqueous granulation solution and a method of tablet granulation | |
| US3876757A (en) | Contraception agent | |
| US6033683A (en) | Method of the manufacture of suppositories | |
| KR20010043408A (ko) | 활성 성분인 가티플록사신, 또는 약제학적으로 적합한이의 염 또는 이의 수화물을 재현 가능하게 방출시키는경구용 의약 제제 | |
| NZ270439A (en) | Solid slow release pharmaceutical composition: carrier is polyethylene glycol and hydrophilic gel-forming polymer | |
| US3826666A (en) | Enteric capsules | |
| AU600712B2 (en) | Pellet-containing pharmaceutical compositions | |
| US4670251A (en) | Microcrystalline tableting excipient derived from whey | |
| JPS585695B2 (ja) | 発泡錠剤の製法 | |
| RO112851B1 (ro) | Derivat de tilidina, procedeu de preparare a acestuia si compozitie farmaceutica continand acest derivat | |
| US2852433A (en) | Method of making enteric medicament compositions | |
| JPH0154015B2 (pl) | ||
| MXPA02002047A (es) | Pildoras de desintegracion rapida en base a quitosana. | |
| US20060073188A1 (en) | Fast-dissolving isotropic expanded microporous composition or structure for pharmaceutical, veterinary, dietetic, food or cosmetic use and method for obtaining same | |
| USRE29102E (en) | Contraception agent | |
| JPS59101420A (ja) | インドメタシンを含有する直腸用調製物 | |
| JPS6115831A (ja) | 速崩壊性ゼラチン硬カプセル | |
| CA2178220C (fr) | Nouveau procede de fabrication de suppositoires |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: TECHNI-PHARMA, FRANCE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:NOTE-SIMMONNARD, AXELLE;SIRITO, ALAIN;REEL/FRAME:008405/0234 Effective date: 19960509 |
|
| STCF | Information on status: patent grant |
Free format text: PATENTED CASE |
|
| FPAY | Fee payment |
Year of fee payment: 4 |
|
| FPAY | Fee payment |
Year of fee payment: 8 |
|
| FPAY | Fee payment |
Year of fee payment: 12 |